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HRID 253245作成日:2026年10月25日

Acetonitrile → Methyl 3,4-bis(2-methoxyethoxy)benzoate

https://huagongshe.com/reaction/253245

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物2-Bromoethyl methyl etherHCID 80972—
反応物Methyl 3,4-DihydroxybenzoateHCID 287064—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3,4-bis(2-methoxyethoxy)benzoateHCID 4510817565%

反応手順

To a mixture of methyl 3,4-dihydroxybenzoate (1.0 g, 6.0 mmol), potassium carbonate (3.3 g, 23.8 mmol) and acetonitrile (30 mL) was added 1-bromo-2-(methyloxy)ethane(1.7 mL, 17.9 mmol). The resulting mixture was heated at reflux 18 hour. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (100 mL), filtered and concentrated. The residue was then diluted with ethyl acetate (100 mL) and washed with 5% sodium hydroxide solution, water and brine (100 mL each), dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (silica gel, 30%-50% ethyl acetate-hexane) to provide methyl 3,4-bis{[2-(methyloxy)ethyl]oxy}benzoate (1.1 g, 3.9 mmol, 65% yield). 1H NMR (400 MHz, CDCl3): 7.65-7.63 (d, 1H), 7.55 (s, 1H), 6.90-6.88 (d, 1H), 4.21-4.18 (m, 4H), 3.87 (s, 3H), 3.80-3.77 (m, 4H), 3.45 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872014B2
出典データセットuspto-grants-2011_01
ORD IDord-9e68aa20b2194111be2538aea8212cfb
出典メモuspto-grants-2011_01